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Published on: June 3, 2016
Chronic high-fat feeding and prolonged fasting in liver-specific ANGPTL4 knockout mice
Kathryn M Spitler1, Shwetha K Shetty1, Emily M Cushing1
1Department of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa, Iowa City, Iowa.
Abstract:
Obesity is associated with dyslipidemia, ectopic lipid deposition, and insulin resistance. In mice, the global or adipose-specific loss of function of the protein angiopoietin-like 4 (ANGPTL4) leads to decreased plasma triglyceride levels, enhanced adipose triglyceride uptake, and protection from high-fat diet (HFD)-induced glucose intolerance. ANGPTL4 is also expressed highly in the liver, but the role of liver-derived ANGPTL4 is unclear. The goal of this study was to determine the contribution of hepatocyte ANGPTL4 to triglyceride and glucose homeostasis in mice during a high-fat diet challenge. We generated hepatocyte-specific ANGPTL4 deficient (Angptl4LivKO) mice, fed them a 60% kcal/fat diet (HFD) for 6 mo and assessed triglyceride, liver, and glucose metabolic phenotypes. We also explored the effects of prolonged fasting on Angptl4LivKO mice. The loss of hepatocyte-derived ANGPTL4 led to no major changes in triglyceride partitioning or lipoprotein lipase activity compared with control mice. Interestingly, although there was no difference in fasting plasma triglyceride levels after a 6 h fast, after an 18-h fast, normal chow diet-fed Angptl4LivKO mice had lower triglyceride levels than control mice. On a HFD, Angptl4LivKO mice initially showed no difference in glucose tolerance and insulin sensitivity, but improved glucose tolerance emerged in these mice after 6 mo on HFD. Our data suggest that hepatocyte ANGPTL4 does not directly regulate triglyceride partitioning, but that loss of liver-derived ANGPTL4 may be protective from HFD-induced glucose intolerance and influence plasma triglyceride (TG) metabolism during prolonged fasting.NEW & NOTEWORTHY1) Angiopoietin-like 4 deficiency in hepatocytes (Angptl4LivKO) does not improve triglyceride phenotypes during high-fat feeding. 2) Angptl4LivKO mice have improved glucose tolerance after chronic high-fat diet. 3) Angptl4LivKO mice have decreased fasting plasma triglyceride levels after an 18-h fast, but not after a 6-h fast.
Insights
Loss of liver angiopoietin-like 4 (ANGPTL4) in mice did not alter triglyceride levels during high-fat feeding but improved glucose tolerance. Hepatocyte ANGPTL4 deficiency also impacted triglyceride metabolism during prolonged fasting.
Area of Science:
- Metabolic research
- Endocrinology
- Molecular biology
Background:
- Obesity is linked to dyslipidemia, ectopic lipid deposition, and insulin resistance.
- Angiopoietin-like 4 (ANGPTL4) influences triglyceride metabolism, but the role of liver-derived ANGPTL4 is not fully understood.
Purpose of the Study:
- To investigate the contribution of hepatocyte ANGPTL4 to triglyceride and glucose homeostasis in mice under high-fat diet (HFD) conditions.
- To assess the impact of liver-specific ANGPTL4 deficiency on metabolic phenotypes during prolonged fasting.
Main Methods:
- Generation of hepatocyte-specific ANGPTL4 deficient (Angptl4^LivKO) mice.
- Feeding mice a 60% kcal/fat diet (HFD) for 6 months.
- Assessment of triglyceride levels, glucose tolerance, insulin sensitivity, and lipoprotein lipase activity.
Main Results:
- Hepatocyte ANGPTL4 deficiency did not significantly alter triglyceride partitioning or lipoprotein lipase activity during HFD.
- Angptl4^LivKO mice exhibited improved glucose tolerance after 6 months on HFD.
- Lower fasting plasma triglyceride levels were observed in Angptl4^LivKO mice after an 18-hour fast, but not after a 6-hour fast.
Conclusions:
- Hepatocyte ANGPTL4 does not appear to directly regulate triglyceride partitioning.
- Loss of liver-derived ANGPTL4 may offer protection against HFD-induced glucose intolerance.
- Hepatocyte ANGPTL4 influences plasma triglyceride metabolism during prolonged fasting.

